Anilinopyridines as inhibitors of fak

US20100317663A1Inactive Publication Date: 2010-12-16GLAXO SMITHKLINE LLC

Patent Information

Authority / Receiving Office
US · United States
Current Assignee / Owner
GLAXO SMITHKLINE LLC
Publication Date
2010-12-16
Estimated Expiration
Not applicable · inactive patent

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Abstract

The present invention relates to a compound of formula (I):or a pharmaceutically acceptable salt thereof, wherein R1-R4, Q, Z, r, and p are as defined herein. Compounds of the present invention are useful in the treatment of diseases associated with FAK overexpression, including proliferative diseases.
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Description

[0001] This invention relates to a class of anilinopyridines that inhibit Focal Adhesion Kinase (FAK), as well as compositions thereof. Compounds of the present invention are useful in the treatment of proliferative diseases.

[0002] Tyrosine kinases play an important role in the regulation of many cell processes including cell proliferation, cell survival, and cell migration. It is known that certain tyrosine kinases become activated by mutation or are abnormally expressed in many human cancers. For example, the epidermal growth factor receptor (EGFR) is found mutated and / or overexpressed in breast, lung, brain, squamous cell, gastric, and other human cancers. Selective inhibitors of the tyrosine kinase activity of EGFR have been shown to be of clinical value in treatment of cancers with mutated and / or overexpressed EGFR. Thus, selective inhibitors of particular tyrosine kinases are useful in the treatment of proliferative diseases such as cancer.

[0003] FAK (encoded by the gene PTK2) is...

Claims

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